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WorldTraining

Which data and systems are subject to 21 CFR Part 11


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Who should attend?

QC Laboratory Staff Managers

Details

Overview:
This webinar demystifies Part 11, and get you on the right track for
using electronic records and signatures to greatly increase
productivity.

Areas Covered in the Session:
Ensure data integrity, security, and protect intellectual property
Understand the current computer system industry standards for
security, data transfer, and audit trails
Electronic signatures, digital pens, and biometric signatures
SOPs required for the IT infrastructure
Product features to look for when purchasing COTS software

Who Will Benefit:
Quality Assurance
Quality Control
Laboratory Staff
Managers
GMP, GCP, GLP Professionals

Speaker Profile:
David Nettleton, is an FDA Compliance Specialist for 21 CFR Part
11, HIPAA, and Computer System Validation. His latest book is
"Risk Based Software Validation - Ten easy Steps" that relates to
the development, purchase, installation, operation and maintenance
of computerized systems used in regulated applications.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

http://www.compliance4all.com/control/w_product/~product_id=501918LIVE?channel=pharmiweb_Jun_2018_SEO

Prices

One Dial-in One Attendee Price: $150.00

Contact

Event Manager
support@compliance4all.com

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